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首页> 外文期刊>Infection and immunity >Host defenses in murine malaria: induction of a protracted state of immunity with a formalin-killed Plasmodium berghei blood parasite vaccine.
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Host defenses in murine malaria: induction of a protracted state of immunity with a formalin-killed Plasmodium berghei blood parasite vaccine.

机译:鼠类疟疾中的宿主防御:用福尔马林杀死的伯氏疟原虫血液寄生虫疫苗诱导持久的免疫状态。

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Random-bred mice were immunized with a nonliving antigen prepared from mixed-blood forms of Plasmodium berghei, strain NYU-2, in combination with Corynebacterium parvum and/or living BCG. A high proportion of intravenously immunized mice survived virulent challenge, but subcutaneous vaccination was less effective. Vaccinated mice developed a patent infection after challenge similar to that observed in normal controls. However, between days 12 to 20 postchallenge, infections in some vaccinated mice became subpatent, whereas infections in all normal controls progressed until death. The incidence of recrudescent infection was low and, eventually, a state of sterile immunity was established. The capacity of vaccinated mice to withstand P. berghei challenge was sustained at a fairly stable level for the 6-month period of observation. Mice that had survived a primary infection with P. berghei almost completely suppressed a second and larger challenge with the same organism.
机译:用由伯氏疟原虫混合株形式NYU-2的混合血形式制备的非活体抗原与小棒杆菌和/或活卡介苗联合免疫小鼠。很大一部分经静脉免疫的小鼠在毒性攻击中存活下来,但皮下接种效果较差。接种疫苗的小鼠在攻击后发生了专利感染,类似于在正常对照中观察到的。但是,在攻击后第12天到第20天之间,某些疫苗接种小鼠的感染变为亚专利,而所有正常对照的感染都进展到死亡。复发性感染的发生率低,最终建立了无菌免疫状态。在六个月的观察期内,接种疫苗的小鼠抵抗伯氏疟原虫攻击的能力维持在相当稳定的水平。在伯氏疟原虫的初次感染中幸存下来的小鼠几乎完全抑制了同一生物的第二次更大的攻击。

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